The Scottish Aortic Stenosis LongiTudinal Imaging and biomarkeR (SALTIRE) Programme

Status: Recruiting
Location: See location...
Intervention Type: Radiation
Study Type: Observational
SUMMARY

The goal of this observational study is to understand the processes of what causes and accelerates the disease progress in aortic stenosis and following aortic valve replacement. Participants will undergo transthoracic echocardiography every 6 months, with annual visits for state-of-the-art scanning techniques including positron-emission tomography combined with computed tomography or magnetic resonance imaging with radiotracers designed to look at disease processes including fibrosis, calcification, inflammation and thrombosis activity.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 50
Healthy Volunteers: t
View:

• Male or female aged \>50 years

• Provision of informed consent prior to any study specific procedures

• Patients with bioprosthetic aortic valve replacements, including both surgically and transcatheter implanted valves

• Patients with severe aortic stenosis (peak velocity \>4.0 m/s; previously recruited patients)

• Patients with moderate aortic stenosis (peak velocity 3.0-4.0 m/s; new prospectively recruited patients)

• Patients with mild aortic stenosis (peak velocity 2.5-2.9 m/s; new prospectively recruited patients)

• Patients with aortic sclerosis (tri-leaflet thickened aortic valve with no obstruction of ventricular outflow)

• Age and sex-matched healthy volunteers

Locations
Other Locations
United Kingdom
University of Edinburgh
RECRUITING
Edinburgh
Contact Information
Primary
Neil Craig
neil.craig@ed.ac.uk
07383558066
Backup
David Newby
d.e.newby@ed.ac.uk
Time Frame
Start Date: 2023-05-22
Estimated Completion Date: 2028-05-22
Participants
Target number of participants: 300
Treatments
Aortic Stenosis
Participants with Aortic Stenosis across the spectrum of disease severity
Aortic Valve Replacement
Participants who have previously undergone aortic valve replacement
Healthy Volunteers
Healthy Volunteers for the purposes of case-control analysis
Related Therapeutic Areas
Sponsors
Leads: University of Edinburgh

This content was sourced from clinicaltrials.gov